Canonical Allele Identifier: PA2825112678
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072127
ClinVar RCV Id: RCV004012157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Cys1411Tyr
CA389040413
NM_000257.4:c.4232G>A